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      Identification of a cold receptor reveals a general role for TRP channels in thermosensation.

      Nature

      Xenopus laevis, cytology, Trigeminal Ganglion, physiology, Thermoreceptors, TRPM Cation Channels, Sequence Homology, Amino Acid, Rats, Sprague-Dawley, Rats, Neurons, Afferent, chemistry, Neoplasm Proteins, Molecular Sequence Data, metabolism, Menthol, genetics, Ion Channels, Gene Expression, Electrophysiology, DNA, Complementary, Cold Temperature, Cloning, Molecular, Cells, Cultured, Calcium Channels, Calcium, Animals, Amino Acid Sequence

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          Abstract

          The cellular and molecular mechanisms that enable us to sense cold are not well understood. Insights into this process have come from the use of pharmacological agents, such as menthol, that elicit a cooling sensation. Here we have characterized and cloned a menthol receptor from trigeminal sensory neurons that is also activated by thermal stimuli in the cool to cold range. This cold- and menthol-sensitive receptor, CMR1, is a member of the TRP family of excitatory ion channels, and we propose that it functions as a transducer of cold stimuli in the somatosensory system. These findings, together with our previous identification of the heat-sensitive channels VR1 and VRL-1, demonstrate that TRP channels detect temperatures over a wide range and are the principal sensors of thermal stimuli in the mammalian peripheral nervous system.

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          Journal
          10.1038/nature719
          11882888

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